Kozhukhov A N, Meĭren D V, Gilev A P
Biull Eksp Biol Med. 1977 Jun;83(6):734-6.
The pharmacokinetics of phthorafur-2-14C (Ph) was investigated after its intravenous injection to rats with Walker carcinosarcoma. The blood plasma level of Ph-2-14C and its metabolites proved to decrease in to a three-phase process. The content of the agent in the tissues decreased in the following sequence: the kidney, small intestine, tumour, stomach, muscle, heart, liver, lungs, spleen, brain and fat. The tumour was observed to contain Ph-2-14C and endogenous metabolite 5-phthoruracil-2-14C. Excretion of the agent continued for 48 hrs, 52.2% of the administered dose being eliminated via the urinary tract, 30% as 14CO2, and 0.8% in feces.
将含有Walker癌肉瘤的大鼠静脉注射phthorafur - 2 - 14C(Ph)后,对其药代动力学进行了研究。结果表明,血浆中Ph - 2 - 14C及其代谢产物的水平呈三相下降过程。该药物在组织中的含量按以下顺序降低:肾脏、小肠、肿瘤、胃、肌肉、心脏、肝脏、肺、脾脏、大脑和脂肪。观察到肿瘤中含有Ph - 2 - 14C和内源性代谢产物5 - phthoruracil - 2 - 14C。药物排泄持续48小时,给药剂量的52.2%通过尿路排出,30%以14CO2形式排出,0.8%通过粪便排出。